ENST00000324041.6:c.397C>G
MANE Select
|
ENSP00000326159.1:p.Arg133Gly
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ENST00000324041.5:c.397C>G
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ENSP00000326159.1:p.Arg133Gly
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ENST00000431178.2:c.250C>G
|
ENSP00000399448.2:p.Arg84Gly
|
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ENST00000593885.1:c.112C>G
|
ENSP00000469769.1:p.Arg38Gly
|
|
ENST00000596876.1:n.316C>G
|
|
|
ENST00000598305.5:c.112C>G
|
ENSP00000469963.1:p.Arg38Gly
|
|
ENST00000599865.5:n.250C>G
|
|
|
ENST00000602148.1:c.409C>G
|
ENSP00000472091.1:n.409C>G
|
|
NM_001302961.1:c.112C>G
|
NP_001289890.1:p.Arg38Gly
|
|
NM_004917.4:c.397C>G
|
NP_004908.4:p.Arg133Gly
|
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NR_126566.1:n.390C>G
|
|
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XM_005259441.3:c.112C>G
|
XP_005259498.2:p.Arg38Gly
|
|
XM_011527545.1:c.397C>G
|
XP_011525847.1:p.Arg133Gly
|
|
XM_011527546.1:c.397C>G
|
XP_011525848.1:p.Arg133Gly
|
|
XM_011527547.1:c.250C>G
|
XP_011525849.1:p.Arg84Gly
|
|
XM_005259441.4:c.112C>G
|
XP_005259498.2:p.Arg38Gly
|
|
XM_011527545.3:c.397C>G
|
XP_011525847.1:p.Arg133Gly
|
|
XM_011527546.2:c.397C>G
|
XP_011525848.1:p.Arg133Gly
|
|
NM_001302961.2:c.112C>G
|
NP_001289890.1:p.Arg38Gly
|
|
NR_126566.2:n.390C>G
|
|
|
NM_004917.5:c.397C>G
MANE Select
|
NP_004908.4:p.Arg133Gly
|
|